Canonical Allele Identifier: CA7457502

Gene: FMN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.33153033T>G , CM000677.2:g.33153033T>G	GRCh38
NC_000015.9:g.33445234T>G , CM000677.1:g.33445234T>G	GRCh37
NC_000015.8:g.31232526T>G	NCBI36
NG_042863.1:g.46701A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616417.5:c.1867+15A>C MANE Select	ENSP00000479134.1:n.1867+15A>C
ENST00000674090.1:n.169+27165A>C
ENST00000320930.7:c.1867+15A>C	ENSP00000325166.7:n.1867+15A>C
ENST00000559047.5:c.1867+15A>C	ENSP00000454047.1:n.1867+15A>C
ENST00000561249.5:c.1867+15A>C	ENSP00000453443.1:n.1867+15A>C
ENST00000616417.4:c.1867+15A>C	ENSP00000479134.1:n.1867+15A>C
NM_001277313.1:c.1867+15A>C	NP_001264242.1:n.1867+15A>C
NM_001277314.1:c.1867+15A>C	NP_001264243.1:n.1867+15A>C
XM_011521504.1:c.1867+15A>C	XP_011519806.1:n.1867+15A>C
XM_011521505.1:c.1867+15A>C	XP_011519807.1:n.1867+15A>C
XM_011521506.1:c.1867+15A>C	XP_011519808.1:n.1867+15A>C
XM_011521507.1:c.1867+15A>C	XP_011519809.1:n.1867+15A>C
XM_011521508.1:c.1867+15A>C	XP_011519810.1:n.1867+15A>C
XM_011521509.1:c.217+27165A>C	XP_011519811.1:n.217+27165A>C
XM_011521504.3:c.1867+15A>C	XP_011519806.1:n.1867+15A>C
XM_011521505.2:c.1867+15A>C	XP_011519807.1:n.1867+15A>C
XM_011521506.3:c.1867+15A>C	XP_011519808.1:n.1867+15A>C
XM_011521507.2:c.1867+15A>C	XP_011519809.1:n.1867+15A>C
XM_011521509.3:c.217+27165A>C	XP_011519811.1:n.217+27165A>C
XM_017022130.2:c.1867+15A>C	XP_016877619.1:n.1867+15A>C
XM_017022131.1:c.1867+15A>C	XP_016877620.1:n.1867+15A>C
XM_017022133.2:c.213+15A>C	XP_016877622.1:n.213+15A>C
XM_017022135.2:c.213+15A>C	XP_016877624.1:n.213+15A>C
NM_001277313.2:c.1867+15A>C MANE Select	NP_001264242.1:n.1867+15A>C
NM_001277314.2:c.1867+15A>C	NP_001264243.1:n.1867+15A>C